Craniofacial Dysostosis
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.
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Subheadings:
Tree Number(s): C05.116.099.370.231, C05.660.207.231, C16.131.621.207.231
MeSH Unique ID: D003394
Entry Terms:
- Dysostosis, Craniofacial
- Craniofacial Dysostoses
- Dysostoses, Craniofacial
- Craniofacial Dysarthrosis
- Craniofacial Dysarthroses
- Dysarthroses, Craniofacial
- Dysarthrosis, Craniofacial
- Craniofacial Dysostosis Syndrome
- Craniofacial Dysostosis Syndromes
- Crouzon Disease
- Crouzon's Disease
- Crouzons Disease
- Crouzon Syndrome
- Crouzon Craniofacial Dysostosis
- Craniofacial Dysostosis, Crouzon
- Craniofacial Dysostosis Type 1
- Craniofacial Dysostosis, Type I
See Also: